Variant report

Variant	nsv896933
Chromosome Location	chr11:5402315-5440620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:245)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:5410351-5410419	K562	blood:	n/a	n/a
2	CTCF	chr11:5411626-5411668	LNCaP	prostate:	n/a	n/a
3	CTCF	chr11:5432429-5432471	Medullo	brain:	n/a	n/a
4	CTCF	chr11:5411516-5411736	K562	blood:	n/a	n/a
5	CTCF	chr11:5402034-5402315	ProgFib	skin:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
6	CTCF	chr11:5411600-5411750	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr11:5411576-5411704	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr11:5411540-5411690	GM06990	blood:	n/a	n/a
9	CTCF	chr11:5401933-5402390	IMR90	lung:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
10	CTCF	chr11:5401938-5402355	MCF-7	breast:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
11	CTCF	chr11:5411540-5411690	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr11:5402625-5402649	GM10266	blood:	n/a	n/a
13	CTCF	chr11:5411500-5411650	HCFaa	heart:	n/a	n/a
14	CTCF	chr11:5411580-5411730	HCT-116	colon:	n/a	n/a
15	CTCF	chr11:5401943-5402334	A549	lung:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
16	CTCF	chr11:5402600-5402750	GM12872	blood:	n/a	n/a
17	CTCF	chr11:5411520-5411670	GM12865	blood:	n/a	n/a
18	CTCF	chr11:5402620-5402770	GM06990	blood:	n/a	n/a
19	CTCF	chr11:5411520-5411670	GM12864	blood:	n/a	n/a
20	CTCF	chr11:5402400-5402550	GM12875	blood:	n/a	n/a
21	CTCF	chr11:5411680-5411830	A549	lung:	n/a	n/a
22	CTCF	chr11:5401971-5402373	H1-hESC	embryonic stem cell:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
23	CTCF	chr11:5411600-5411750	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr11:5411340-5411490	GM12866	blood:	n/a	n/a
25	CTCF	chr11:5411520-5411670	HEK293	kidney:	n/a	n/a
26	CTCF	chr11:5411540-5411690	GM12871	blood:	n/a	n/a
27	CTCF	chr11:5411600-5411750	BJ	skin:	n/a	n/a
28	CTCF	chr11:5411540-5411690	GM12878	blood:	n/a	n/a
29	CTCF	chr11:5402030-5402316	LNCaP	prostate:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173
30	CTCF	chr11:5411520-5411670	GM12872	blood:	n/a	n/a
31	CTCF	chr11:5411520-5411670	HRE	kidney:	n/a	n/a
32	CTCF	chr11:5432422-5432428	Medullo	brain:	n/a	n/a
33	CTCF	chr11:5411587-5411677	HepG2	liver:	n/a	n/a
34	CTCF	chr11:5411560-5411710	GM12873	blood:	n/a	n/a
35	CTCF	chr11:5411540-5411690	GM12875	blood:	n/a	n/a
36	CTCF	chr11:5402440-5402590	AG10803	skin:	n/a	n/a
37	CTCF	chr11:5411560-5411710	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr11:5402660-5402810	GM12866	blood:	n/a	n/a
39	CTCF	chr11:5411520-5411670	GM12878	blood:	n/a	n/a
40	CTCF	chr11:5411500-5411650	GM12871	blood:	n/a	n/a
41	CTCF	chr11:5402520-5402670	GM12873	blood:	n/a	n/a
42	CTCF	chr11:5411540-5411690	AG04450	lung:	n/a	n/a
43	CTCF	chr11:5411598-5411668	LNCaP	prostate:	n/a	n/a
44	CTCF	chr11:5411500-5411650	K562	blood:	n/a	n/a
45	CTCF	chr11:5411540-5411690	GM12872	blood:	n/a	n/a
46	CTCF	chr11:5411520-5411670	GM12874	blood:	n/a	n/a
47	CTCF	chr11:5411640-5411790	HAc	cerebellar:	n/a	n/a
48	CTCF	chr11:5411500-5411650	AG04450	lung:	n/a	n/a
49	CTCF	chr11:5411460-5411610	RPTEC	kidney:	n/a	n/a
50	CTCF	chr11:5402014-5402334	GM19238	blood:	n/a	chr11:5402153-5402174 chr11:5402159-5402175 chr11:5402161-5402171 chr11:5402164-5402173 chr11:5402158-5402176 chr11:5402160-5402173

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5433817-5433867	IMR90	lung:	fetal
2	chr11:5433817-5433867	IMR90	lung:	fetal
3	chr11:5410452-5410502	PrEC	prostate:	n/a
4	chr11:5410452-5410502	HCM	heart:	n/a
5	chr11:5410452-5410502	K562	blood:	n/a
6	chr11:5410053-5410103	RPTEC	kidney:	n/a
7	chr11:5410053-5410103	ovcar-3	ovarian:	n/a
8	chr11:5433817-5433867	BE2_C	brain:	n/a
9	chr11:5408788-5408838	Hepatocyte	liver:	n/a
10	chr11:5408788-5408838	PANC-1	pancreas:	n/a
11	chr11:5410452-5410502	T-47D	breast:	n/a
12	chr11:5408788-5408838	AG04449	skin:	fetal
13	chr11:5433817-5433867	HCM	heart:	n/a
14	chr11:5410053-5410103	MCF-7	breast:	n/a
15	chr11:5408788-5408838	HepG2	liver:	n/a
16	chr11:5433817-5433867	SK-N-SH	brain:	n/a
17	chr11:5433817-5433867	PANC-1	pancreas:	n/a
18	chr11:5433817-5433867	NH-A	brain:	n/a
19	chr11:5410452-5410502	HEEpiC	esophagus:	n/a
20	chr11:5408788-5408838	SK-N-MC	brain:	n/a
21	chr11:5408788-5408838	GM12878	blood:	n/a
22	chr11:5410053-5410103	HCPEpiC	choroid plexus:	n/a
23	chr11:5410452-5410502	Hela-S3	cervix:	n/a
24	chr11:5410452-5410502	CMK	blood:	n/a
25	chr11:5433817-5433867	GM06990	blood:	n/a
26	chr11:5433817-5433867	CMK	blood:	n/a
27	chr11:5408788-5408838	HEEpiC	esophagus:	n/a
28	chr11:5410452-5410502	PFSK-1	brain:	n/a
29	chr11:5410053-5410103	HRE	kidney:	n/a
30	chr11:5410053-5410103	Hela-S3	cervix:	n/a
31	chr11:5408788-5408838	K562	blood:	n/a
32	chr11:5408788-5408838	SK-N-SH	brain:	n/a
33	chr11:5410053-5410103	NB4	blood:	n/a
34	chr11:5410053-5410103	HEK293	kidney:	embryo
35	chr11:5408788-5408838	ECC-1	luminal epithelium:	n/a
36	chr11:5408788-5408838	GM06990	blood:	n/a
37	chr11:5410452-5410502	GM06990	blood:	n/a
38	chr11:5410452-5410502	HCPEpiC	choroid plexus:	n/a
39	chr11:5410452-5410502	Jurkat	blood:	n/a
40	chr11:5410452-5410502	NB4	blood:	n/a
41	chr11:5410452-5410502	HRCEpiC	kidney:	n/a
42	chr11:5408788-5408838	Caco-2	colon:	n/a
43	chr11:5408788-5408838	NT2-D1	testis:	n/a
44	chr11:5410452-5410502	RPTEC	kidney:	n/a
45	chr11:5410452-5410502	PANC-1	pancreas:	n/a
46	chr11:5408788-5408838	ProgFib	skin:	n/a
47	chr11:5408788-5408838	HRPEpiC	eye:	n/a
48	chr11:5410452-5410502	NH-A	brain:	n/a
49	chr11:5408788-5408838	HRCEpiC	kidney:	n/a
50	chr11:5408788-5408838	HCF	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
2	11:5218976-5222789..11:5425882-5426881	GM12878	blood:
3	chr11:5404523..5406570-chr11:5525377..5527235,2	K562	blood:
4	11:5250847-5268367..11:5398331-5406514	Hela-S3	cervix:
5	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
6	11:5398331-5406514..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
7	11:5250847-5268367..11:5406514-5407716	Hela-S3	cervix:
8	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
9	11:5218976-5222789..11:5398331-5406514	GM12878	blood:
10	11:5018576-5020673..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
11	chr11:5403316..5405023-chr11:5406492..5408561,2	K562	blood:
12	11:5421776-5424121..11:5425882-5426881	GM12878	blood:
13	11:5243048-5250847..11:5398331-5406514	H1-hESC	embryonic stem cell:	embryo
14	11:4778081-4789138..11:5398331-5406514	Hela-S3	cervix:
15	11:5243048-5250847..11:5425882-5426881	GM12878	blood:
16	11:4778081-4789138..11:5425882-5426881	H1-hESC	embryonic stem cell:	embryo
17	11:5398331-5406514..11:5707362-5712027	K562	blood:
18	chr11:5403316..5405023-chr11:5406492..5408561,2	K562	blood:
19	11:5146608-5154908..11:5398331-5406514	GM12878	blood:
20	chr11:5415584..5416428-chr20:41864268..41865032,2	MCF-7	breast:
21	chr11:5405070..5407795-chr11:5524807..5526877,2	K562	blood:
22	chr11:5403286..5405023-chr11:5406097..5408561,2	K562	blood:
23	chr11:5403286..5405023-chr11:5406097..5408561,2	K562	blood:
24	chr11:5225752..5226648-chr11:5401460..5402799,4	MCF-7	breast:
25	chr11:5402164..5402741-chr11:5497230..5497968,2	MCF-7	breast:
26	chr11:5145230..5145917-chr11:5402049..5402594,2	MCF-7	breast:
27	11:5398331-5406514..11:5700314-5707362	GM12878	blood:
28	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:

No data

Variant related genes	Relation type
OR51M1	TF binding region
OR51J1	TF binding region
OR51Q1	TF binding region
OR51M1	CpG island
OR51J1	CpG island
OR51Q1	CpG island
ENSG00000223609	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000184321	chromatin interactions
ENSG00000205494	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000229988	chromatin interactions

Extended variants
information (count: 2203 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2203 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11037120	chr11:5402315-5402316	Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146546272	chr11:5402339-5402340	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
3	rs111996173	chr11:5402342-5402343	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
4	rs375782652	chr11:5402346-5402347	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
5	rs564594437	chr11:5402349-5402350	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
6	rs528276295	chr11:5402370-5402371	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
7	rs546809998	chr11:5402380-5402381	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
8	rs568256975	chr11:5402383-5402384	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
9	rs535789780	chr11:5402388-5402389	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
10	rs113307514	chr11:5402389-5402390	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
11	rs145199859	chr11:5402390-5402391	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
12	rs563242544	chr11:5402397-5402398	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
13	rs199629139	chr11:5402398-5402399	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
14	rs12362422	chr11:5402399-5402400	Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
15	rs542416527	chr11:5402401-5402402	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
16	rs28695888	chr11:5402402-5402403	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
17	rs71050492	chr11:5402404-5402405	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs61548181	chr11:5402405-5402406	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs71975655	chr11:5402406-5402407	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs74573388	chr11:5402417-5402418	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs113920235	chr11:5402441-5402442	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs116336900	chr11:5402469-5402470	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs182363470	chr11:5402495-5402496	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs116943508	chr11:5402500-5402501	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs144123948	chr11:5402538-5402539	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs574939123	chr11:5402552-5402553	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs2723373	chr11:5402554-5402555	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563842644	chr11:5402562-5402563	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs2736543	chr11:5402564-5402565	Enhancers Strong transcription	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs546249913	chr11:5402615-5402616	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs373637245	chr11:5402628-5402629	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs2647546	chr11:5402639-5402640	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs528639981	chr11:5402649-5402650	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs2736542	chr11:5402657-5402658	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs561872639	chr11:5402674-5402675	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
36	rs529085806	chr11:5402680-5402681	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
37	rs550814896	chr11:5402701-5402702	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs568831345	chr11:5402705-5402706	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs139984112	chr11:5402764-5402765	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs550996425	chr11:5402792-5402793	Enhancers Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs78509418	chr11:5402834-5402835	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs77040155	chr11:5402836-5402837	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs187908295	chr11:5402868-5402869	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs574943812	chr11:5402881-5402882	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs535692405	chr11:5402882-5402883	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs191936481	chr11:5402932-5402933	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs576044127	chr11:5402940-5402941	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs138699277	chr11:5402949-5402950	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs6578626	chr11:5402970-5402971	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs564520927	chr11:5402976-5402977	Enhancers Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5401000-5404400	Strong transcription	K562	blood
2	chr11:5402400-5405000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:5404400-5407400	Weak transcription	K562	blood
4	chr11:5404600-5405400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr11:5404600-5405600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr11:5404600-5406000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:5404600-5406400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:5404800-5405400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr11:5405000-5405400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:5405000-5405400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr11:5405000-5405400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5405000-5405400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:5405000-5405800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:5405000-5405800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:5405000-5405800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr11:5405000-5406000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr11:5405400-5406800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:5405400-5408400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr11:5405400-5408600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr11:5405600-5408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr11:5405800-5408400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:5405800-5408800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:5406000-5408400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr11:5406000-5410200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr11:5406800-5408600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:5407400-5409200	Strong transcription	K562	blood
27	chr11:5408400-5410200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr11:5408400-5410200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr11:5408400-5410400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr11:5408600-5409600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:5408600-5410000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr11:5408600-5410200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:5408800-5410600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:5409200-5410600	Weak transcription	K562	blood
35	chr11:5409600-5412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:5410200-5410400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr11:5410600-5412600	Strong transcription	K562	blood
38	chr11:5411200-5411400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:5412200-5412400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:5412600-5415000	Weak transcription	K562	blood
41	chr11:5415000-5417000	Strong transcription	K562	blood
42	chr11:5415800-5417000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:5417000-5417400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:5417000-5420000	Weak transcription	K562	blood
45	chr11:5417400-5420800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:5420000-5423000	Strong transcription	K562	blood
47	chr11:5420800-5421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:5422000-5422200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:5423000-5424200	Weak transcription	K562	blood
50	chr11:5424200-5425800	Strong transcription	K562	blood

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